Method for the production of highly pure metallic nano-powders produced thereby

ABSTRACT

The present invention discloses a novel method for the production of metallic nano-powder. This cost-effective, simple process is customized for a full-scale production of metallic nano-powders containing a first metal, and comprising the following of forming an alloy comprising said first metal and at least one soluble metal; applying first thermal treatment in the manner homogenized alloy is obtained; applying a cold work to the homogenized alloy so thin strips are obtained; applying a second thermal treatment to the alloy until a phase composition of predetermined characteristics is obtained; subjecting the said alloy to a leaching agent adapted to effectively leach out the least one soluble metal; filtering and washing the powder; washing the powder; drying the powder; coating the powder with chemicals; and then de-agglomerating the coated powder. The present invention also discloses a cost-effective and highly pure metallic powder produced by the method defined above.

FIELD OF THE INVENTION

The present invention generally relates to a method for the production of highly pure metallic nano-powders and to powders produced thereof. More specifically, the present invention relates to metallic silver, metal elements, copper, platinum, nickel, palladium, titanium, gold, cobalt and blends comprising such metals (alloys) nano-powders wherein the particle size is in the range of 1 to 100 nm.

BACKGROUND OF THE INVENTION

Nano-powders are single or multi-phase polycrystals comprises particles with sizes of 1 to 100 nm in at least one direction. Various methods were suggested in the literature for the production of well-defined nano-powders. Some of them, such as presented in U.S. Pat. No. 6,312,643 to Upadhya et al. are respectively tedious and costly operation, comprises no less then 21 steps, treating the material in all solid, liquid and gas phases; wherein gas is evacuated from one processing chamber to less then 10⁻³ Torr, and then pressed in another processing chamber to at least 10³ psi, heated to some 550° C. etc.

U.S. Pat. No. 6,054,495 to Markowitz et al. presents a powder of un-agglomerated metallic particles, made by making at least four dispersions of surfactants vesicles in the presence of metal ions, and then freeze-drying the obtained lipid phase. This costly method requires the operator to continuously control this very delicate, inflammable, multi-phase and complicated system, decreasing its compatibility with full-scale operations.

U.S. Pat. 5,476,535 to the applicant present a method for the production of nano-powders, especially of silver. This process comprising the steps of (a) forming an aluminum-silver alloy of a specific blend composition; (b) leaching the aluminum ingredient by a series of consequent leaching steps wherein a fresh leaching agent is reacting the treated solid material, providing a gradually porous and homogeneous silver alloy. Ultrasonic oscillations are applied in step (c), disintegrating the agglomerate and enhancing the penetration of the leaching agent into the ever growing porous of the alloy by the application of a plurality of ultrasonic oscillations. The leaching agent is leaving silver agglomerate in step (d), and then the agglomerate is washed and dried in a final step.

According to U.S. Pat. No. 6,012,658 to the applicant, the very same process was used as is to form metal flasks. Thus, the following two main steps were introduced: comminuting the alloys obtained by the aforementioned U.S. Pat. No. 5,476,535 into defined particles, and then faltering the obtained particles into strip-like highly porous alloys of predetermined characteristics.

Thus, there exists a need for cost-effective, simple process customizable for full-scale production of metallic nano-powders and to the valuable products produced thereof.

SUMMARY OF THE INVENTION

It thus the object of the present invention to provide a useful and novel method for the production of metallic nano-powders, comprising the steps: (a) forming an alloy comprising a first metal or metal, preferably silver, copper, platinum, palladium, titanium, nickel, gold, cobalt and blends comprising such metals (alloys), yet not limited to said metals, and at least one another second soluble metal or metals, preferably, yet not limited to aluminum, magnesium, zinc or tin. (b) applying first thermal treatment in the manner homogenized alloy is obtained; (c) applying a cold work to the homogenized alloy so thin strips are obtained; (d) applying a second thermal treatment to the said alloy until a phase composition of predetermined characteristics is obtained; (e) subjecting the said alloy to a leaching agent adapted to effectively leach out the least one soluble metal; (f) filtering and washing the powder; (g) drying the powder; (h) coating the powder with chemicals; and lastly, (i) de-agglomerating the coated powder.

This method is based on gradually single leaching step and plurality of few thermal treatings, avoid using ulrasonic processes, and comprising a novel technique of coating the powder with predetermined chemicals which provides the obtained powder better de-agglomeration properties and de-agglomeration process.

It is another object of the present invention to provide pure metallic powder having particle size of nano scale, produced in the method defined above. More specifically, the aim of the present invention is to introduce a nano-powder comprising about 99.0%-99.6% desired metal and less then 1% soluble metal, having a specific area of about 6 to 25 m² per gram and characterized by an average particle size of about 50 to 100 nm.

DETAILED DESCRIPTION OF THE INVENTION

It is thus in the scope of the present invention to present a useful method for the production of metallic nano-powder of a first metal. Said method if essentially comprising the following at least nine steps:

-   -   i. forming an alloy comprising a first metal and at least one         another second soluble metal;     -   ii. applying first thermal treatment in the manner homogenized         alloy is obtained;     -   iii. applying a cold work to the homogenized alloy so thin         strips are obtained;     -   iv. applying a second thermal treatment to the said alloy until         a phase composition of predetermined characteristics is         obtained;     -   v. subjecting the said alloy to a leaching agent adapted to         effectively leach out the least one soluble metal;     -   vi. filtering and washing the powder;     -   vii. drying the powder;     -   viii. coating the powder with chemicals; and lastly,     -   ix. de-agglomerating the coated powder.

It is acknowledged that while the present invention has been described with the respect to a plurality of few preferred examples, it will be appropriated that many variations, modifications and applications of the invention may be made.

It is hence in the general scope of the present invention, wherein the first metal is selected from atoms of group I, IV, V, VI, VII and VIII of the periodic table of elements. More specifically, said first metal is selected from, copper, nickel, cobalt, titanium, silver, palladium, platinum, gold and iridium. Most particularly, silver is said first metal. In addition, various alloys comprising a blend of the said silver and at least one other metal, selected from atoms of group I, IV, V, VI, VII and VIII of the periodic table of elements. More specifically, cooper, aluminum, nickel, cobalt, titanium, palladium, platinum, gold, iridium or—any mixture thereof is suitable to be comprised in the aforementioned alloy.

In addition, it is also in the scope of the invention, wherein the at least one soluble metal is selected from aluminum, zinc, magnesium, tin, copper and silver. In one embodiment of the present invention is wherein the concentration of the at least one soluble metal is near saturation. Most specifically, the present invention relates thus to a method to produce a nano-powder, wherein silver is the first metal and aluminum is the soluble metal.

It is acknowledged that the preferred concentration of the soluble metal ingredient of the said processed alloy is in the range between 5 to 90% w/w.

As said above, the method according to the present invention comprises at least one step of leaching. Suitable leaching agents are preferably selected from sodium hydroxide, potassium hydroxide, acetic acid, hydrochloric acid, formic acid, sulfuric acid, hydrofluoric acid, nitric acid or any combination thereof. It is acknowledged that a sequent of few leaching steps useful to extract the soluble metal from the alloy, wherein in each leaching step comprising different leaching agent at possibly different concentration.

The hereto-defined method may additionally comprise at least one step of surface cleansing wherein the obtained strips are treated by means of at least one cleaning agent. Those cleansing agents are preferably selected from nitric acid, potassium hydroxide, sodium hydroxide or a mixture thereof.

According to the present invention, the term ‘heat treatment’ is defined as any heating, cooling, smelting, fusing or melting, amalgamating, liquidating, sustaining a substrate in a predetermined temperature and for a predetermined period or any combination thereof. It is thus in the scope of the present invention, wherein the temperature ranges of first thermal treatment is about 400° C. for 2 to 4 hours, or alternatively, until a homogenized alloy is obtained. Similarly, According to the present invention, the term ‘cold work’ is defined as any work or force provided on the substrate. This work is selected, yet not limited to pressing, compressing, squashing, mashing, pulverizing, grinding, milling or any combination thereof. Thus, the aforementioned method comprises a step of cold work as defined above, useful for applying the obtained strip a thickness in the range of 0.3 to 1.0 mm or thinner.

In one specific embodiment of the present invention, especially adapted to the family of silver-aluminum alloys, the above mentioned second thermal treatment is adapted to the range of 460° C. to 610° C. Said method according to the present invention may additionally comprising a step of quenching steps, wherein the strips obtained from the oven are to be treated by means of immersing them in cold water, so the predetermined phase composition obtained during the heat treatment is provided.

According to the present invention, sodium hydroxide is a useful leaching agent, adapted to be effective wherein the leaching temperature is between 36° C. to 80° C.

In one specific embodiment of the present invention, silver is the first metal and aluminum is the soluble metal. Here, the concentration of the aforementioned sodium hydroxide is between 25 to 55% (w/w) and the molar ratio of the aluminum to the said sodium hydroxide is between 5 to 6.

The obtained powder is preferably to be filtered and washed by water so pH in the range of 6 to 7 is provided and further wherein at a maximum temperature of 45° C., the powder to a LOD weight ratio is lower 1%.

The present invention relates to various chemical compositions, some of them are wieldy known in the art in their trademark name. Those terms are denoted in the present invention according their definitions introduced in Table 1 below: TABLE 1 The trade name and the chemical name of chemicals utilized in the present invention. Trade name Chemical name Arlacel 60 sorbitan sesquioleate Arlacel 83 sorbitan sesquioleate Brig 30 polyoxyethylene lauryl ester Brij 35 Polyoxylene lauryl ester Cetyl alcohol Hexadecanol Diethylene glycol monolaurate Glyceryl monostearate glyceryl monostearate Lauroglycol propylene glycol monostearate Methocel Methylcellulose Myrj 45 Polyoxyethylene monostearate Myrj 49 Polyoxyethylene monostearate Myrj 52 polyoxyl 40 stearate PEG 400 polyoxyethylene monolaurate PEG 400 monoleate polyoxyethylene monooleate PEG 400 monostearate polyoxyethylene monostearate Pluronic F-68 gelatin Potassium oleate poloxamer Span 20 Sorbitan monolaurate Span 40 sorbitan monopalmitate Span 60 sorbitan monostearate Span 65 sorbitan tristearate Span 80 Sorbitan mono-oleate Span 85 Sorbitan trioleate Tween 20 Polyoxyethylene sorbitan monolaurate Tween 21 polyoxyethylene sorbitan monolaurate Tween 40 polyoxyethylene sorbitan monopalmitate Tween 60 polyoxyethylene sorbitan monostearate Tween 61 polyoxyethylene sorbitan monostearate Tween 65 Polyoxyethylene sorbitan tristearate Tween 80 Polyoxyethylene sorbitan mono-oleate Tween 81 polyoxyethylene sorbitan monooleate Tween 85 Polyoxyethylene sorbitan trioleate sorbic acid 2,4 hexadienoic acid TOPO trioctylphosphine oxide TOP trioctylphosphine T1124 Ammonium salt of poly carboxylic acid

It was stressed above that various chemicals are useful for coating the powder. According to the present invention, chemicals hereby defined, yet not limited to this list, are selected from sorbitan esters, polyoxyethylene esters, alcohols, glycerin, polyglycols, organic acids salts and esters, thiols, phosphines, acrylics and polyesters or any other suitable low molecular weight polymers or combination thereof were found to comprise superior effectively.

Moreover, it is hereby acknowledged that chemicals for coating the powder are admixed to the range of 1 to 5%, weight-by-weight based on the metal. Alternatively, least two different chemicals are to be used for coating the powder. In this case, at least one primary chemical is admixed in the range 1% to 5%, and at least one secondary chemical is admixed in the range of 0.1 to 2.5% weight by weight based on the metal. Table 2 presents an extracted list of useful combinations of both primary and secondary chemicals. TABLE 2 Various combinations of both primary and secondary chemicals useful for coating the powder: Primary Chemical Secondary Chemical Tween 80 Oleic Acid Span 20 Tween 20 Span 60 Hexadecanol Span 65 Tween 20 Span 80 Hexadecanol Span 80 cetyl alcohol Span 20 Oleic Acid Span 20 Octanol Span 60 Glycerin Span 60 Propylene Glyecol Span 65 Tween 20 Span 20 Hexadecanol Glycerin Mono Glycerine Span 60 Glycerine poloxyethylene (23) Span 60 poloxyethylene (4) Span 60 Palmitic Acid Glycerin

It also in the scope of the present invention wherein the method for the production of the said metallic nano-powers additionally comprises the following steps:

-   -   a. dissolving the chemicals in a solvent;     -   b. admixing the dissolved chemicals with the metal powder by an         efficient mean; and then,     -   c. drying the slurry in an oven at low temperature.

The above-mentioned solvent is preferably selected from of low boiling temperature solvent, and more specifically from methanol, ethanol, isopropanol, acetone, water or combination thereof. It is also suggested according to use a ball mill to admixed the dissolved chemicals with the metal powder.

It is also in the scope of the present invention, wherein the said de-agglomeration of the said coated powder is enabled by means of a dry process, using at least one jet mill. Additionally or alternatively, said de-agglomerating of the coated powder is also enabled by means of a wet process, using effective means selected from of any suitable mechanical dispersers, mechanical homogenizes, ultra sonic homogenizes or any combination thereof. In this respect, means selected from, yet not limited to rotor/stator; rotors; dispersing elements; mechanical homogenizers; ultra-sonic homogenizers; ball milling and/or any other suitable de-agglomeration means are acknowledged as useful.

It is well in the scope of the present invention to provide a metallic nano-powder produced by the method as defined above. In general, said metal is selected from the group I, IV, V, VI, VII and VIII of the periodic table of elements. More specifically, the said metal powder is selected from silver, cooper, nickel, cobalt, titanium, silver, palladium, platinum, gold and iridium. In addition, said produced nano-powder comprises metal that is preferably selected from alloys comprising a blend of silver and at least one other metal, selected from atoms of group I, IV, V, VI, VII and VIII of the periodic table of elements.

EXPERIMENTAL

A metallic nano-powder comprising silver, silver-cooper, silver palladium, silver-platinum, and cooper was produced by the method of forming an alloy comprising said first metal and at least one soluble metal, selected from aluminum, zinc and magnesium, applying first thermal treatment in the manner homogenized alloy is obtained; applying a cold work to the homogenized alloy so thin strips are obtained; applying a second thermal treatment to the previously leached alloy until a phase composition of predetermined characteristics is obtained; subjecting the said alloy to a leaching agent (i.e., sodium hydroxide, hydrochloride, formic acid and sulfuric acid) adapted to effectively leach out the least one soluble metal; filtering and washing the powder; drying the powder; coating the powder with chemicals; and then, de-agglomerating the coated powder by various means (e.g., using the commercial available Kinematica or jet mills): TABLE 3 Nine different experiments of producing metallic nano-powders by means of the present invention. Powder First Leaching Exp. Metal Main metal Second metal Auxiliary Leaching Chemical Water Solution No. Alloy Quantity Quantity Metal Quantity Chemical Quantity Quantity Volume 1 Ag 3,000 0 Al 7,000 NaOH 48 KG 144 L 150 L 2 Ag/Cu 2,925 75 Al 12,000 NaOH 48 KG 144 L 150 L 3 Ag/Cu 2,925 75 Al 12,000 NaOH 48 KG 144 L 150 L 4 Ag/Pd 2,940 60 Al 12,000 NaOH 48 KG 144 L 150 L 5 Ag/Pt 2,940 60 Al 12,000 NaOH 48 KG 144 L 150 L 6 Cu 620 0 Al 2,560 NaOH 34 KG 100 L 104 L 7 Cu 50 0 Zn 150 HCl 2 Kg 2 L 4 L HCl 32% 8 Cu 50 0 Mg 150 Formic 2.8 Kg 3.2 L 6 L acid F.A. 85% 9 Cu 100 0 Mg 150 H2SO4 1.2 Kg 4.8 L 6 Kg H2SO4 Second Leaching Powder Deagglomeration Process Exp. Leaching Chemical Water Solution Quantity Chemicals No. Chemical Quantity Quantity Volume after leaching (coating) Technique 1 NaOH 1.6 KG 3.4 L 6.4 L 2880 see table 4 JM 2 NaOH 1.6 KG 3.4 L 6.4 L 2880 see table 4 JM 3 NaOH 1.6 KG 3.4 L 6.4 L 2880 see table 4 Kinematica 4 NaOH 1.6 KG 3.4 L 6.4 L 2880 see table 4 JM 5 NaOH 1.6 KG 3.4 L 6.4 L 2880 see table 4 JM 6 HCl 3 Kg 3.0 L 6.0 L 610 see table 4 JM HCl 32% 7 HCl 0.5 Kg 0.5 L 1 L 49 see table 4 JM HCl 32% 8 HCl 0.5 Kg 0.5 L 1 L 49 see table 4 JM HCl 32% 9 HCl 1 Kg   1 L 2 L 98 see table 4 Kinematica HCl 32%

TABLE 4 Nine different coating systems to produce nano-metal particles according to this invention. De-agglomeration Process Total Exper- Metal Chemicals (coating) Powder iment Alloy Quantities per 1 kg powder Technique yield, % 1 Ag 156 g Span 80; 144 g Cetyl JM 85 Alcohol 2 Ag/Cu 120 g Span 20; 180 g Oleic JM 85 acid 3 Ag/Cu 300 g Tween 80 Kinematica 90 4 Ag/Pd 300 g Span 60 JM 85 5 Ag/Pt 150 g Palmitic acid; 150 g JM 85 Glycerine 6 Cu 300 g Byk 140 JM 90 7 Cu 200 g Span 20; 100 g cetyl JM 90 alcohol 8 Cu 300 g Trioctylphosphine JM 90 Oxide 9 Cu 300 g Octanethiol Kinematica 92 

1-34. (canceled)
 35. A method for producing a metal nano-powder comprising: (a) forming an alloy comprising a first metal and a second metal that is different from the first metal; (b) subjecting the alloy to a leaching agent effective to leach out the second metal and form a metal nano-powder; and (c) coating the metal nano-powder with a chemical reagent to form a coated metal nano-powder.
 36. A method according to claim 35 further comprising thermally treating the alloy prior to leaching.
 37. A method according to claim 36 comprising thermally treating the alloy at a temperature between 460 and 610° C.
 38. A method according to claim 35 further comprising cold working the alloy to create thin strips comprising the alloy prior to leaching.
 39. A method according to claim 38 further comprising thermally treating the alloy prior to cold working.
 40. A method according to claim 39 comprising thermally treating the alloy at a temperature of about 400° C.
 41. A method according to claim 35 wherein the chemical reagent is selected from the group consisting of sorbitan esters, polyoxyethylene esters, alcohols, glycerin, polyglycols, organic acid, organic acid salts, organic acid esters, thiols, phosphines, low molecular weight polymers, and combinations thereof.
 42. A method according to claim 35 further comprising de-agglomerating the coated metal nano-powder using a jet mill.
 43. A method according to claim 35 further comprising de-agglomerating the coated metal nano-powder using a mechanical disperser, a mechanical homogenizer, an ultrasonic homogenizer, or combination thereof.
 44. A method according to claim 35 wherein the first metal is selected from the group consisting of silver, copper, nickel, cobalt, titanium, palladium, platinum, gold, iridium, and combinations thereof.
 45. A method according to claim 35 wherein the second metal is selected from the group consisting of aluminum, zinc, magnesium, tin, copper, and silver.
 46. A method according to claim 35 wherein the leaching agent is selected from the group consisting of sodium hydroxide, potassium hydroxide, and combinations thereof.
 47. A method according to claim 35 wherein the leaching agent is selected from the group consisting of acetic acid, hydrochloric acid, formic acid, sulfuric acid, nitric, acid, hydrofluoric acid, and combinations thereof.
 48. A method according to claim 35 wherein the metal nano-powder comprises an alloy.
 49. A method according to claim 45 wherein the metal nano-powder comprises an alloy of silver and at least one other metal element selected from Group I, Group IV, Group V, Group VI, Group VII, and Group VIII of the Periodic Table of Elements.
 50. A method according to claim 35 comprising coating the metal nano-powder with at least two different chemical reagents.
 51. A method for producing a metal nano-powder comprising: (a) forming an alloy comprising a first metal and a second metal that is different from the first metal; (b) subjecting the alloy to a first thermal treatment to form a thermally treated alloy; (c) cold working the thermally treated alloy to form thin strips comprising the alloy; (d) subjecting the thin strips to a second thermal treatment to form thermally treated thin strips comprising the alloy; (e) subjecting the thermally treated thin strips to a leaching agent effective to leach out the second metal to form a metal nano-powder; (f) washing and drying the metal nano-powder; (g) coating the metal nano-powder with a chemical reagent to form a coated metal nano-powder; and (h) de-agglomerating the coated metal nano-powder.
 52. A coated metal nano-powder prepared according to the method of claim
 35. 53. A coated metal nano-powder prepared according to the method of claim
 51. 